Variant report

Variant	nsv888341
Chromosome Location	chr7:70249358-70316365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:940)
CpG islands
(count:1530)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70258518-70258992	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70264860-70265281	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:70264853-70265265	GM12878	blood:	n/a	n/a
10	BATF	chr7:70264945-70265249	GM12878	blood:	n/a	n/a
11	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
12	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:70264916-70265214	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:70264860-70265214	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:70250727-70250742	A549	lung:	n/a	n/a
16	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
17	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
18	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
22	CEBPB	chr7:70250424-70250609	Hela-S3	cervix:	n/a	chr7:70250526-70250537
23	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
25	CEBPB	chr7:70259112-70259395	HepG2	liver:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
26	CEBPB	chr7:70275675-70275878	K562	blood:	n/a	chr7:70275762-70275779
27	CEBPB	chr7:70250396-70250674	HepG2	liver:	n/a	chr7:70250526-70250537
28	CEBPB	chr7:70258165-70258365	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:70275646-70275979	HepG2	liver:	n/a	chr7:70275762-70275779
30	CEBPB	chr7:70275639-70275877	A549	lung:	n/a	chr7:70275762-70275779
31	CEBPB	chr7:70259155-70259386	K562	blood:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
32	CEBPB	chr7:70275643-70275871	HepG2	liver:	n/a	chr7:70275762-70275779
33	CEBPB	chr7:70259112-70259411	A549	lung:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
34	CEBPB	chr7:70277650-70277842	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
36	CEBPB	chr7:70250444-70250691	MCF-7	breast:	n/a	chr7:70250526-70250537
37	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
38	CEBPB	chr7:70257703-70257833	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:70275577-70275965	HepG2	liver:	n/a	chr7:70275762-70275779
40	CEBPB	chr7:70259127-70259380	IMR90	lung:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
41	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
42	CEBPB	chr7:70254214-70254423	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:70295452-70295643	HepG2	liver:	n/a	chr7:70295552-70295563
44	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
45	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
47	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
48	CEBPB	chr7:70254236-70254480	K562	blood:	n/a	n/a
49	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70256003-70256053	MCF10A-Er-Src	breast:	n/a
2	chr7:70252953-70253003	NHDF-neo	bronchial:	n/a
3	chr7:70311321-70311371	HNPCEpiC	eye:	n/a
4	chr7:70255332-70255382	AoSMC	blood vessel:	n/a
5	chr7:70254810-70254860	HCM	heart:	n/a
6	chr7:70256003-70256053	MCF10A-Er-Src	breast:	n/a
7	chr7:70252953-70253003	NHDF-neo	bronchial:	n/a
8	chr7:70311321-70311371	HNPCEpiC	eye:	n/a
9	chr7:70255332-70255382	AoSMC	blood vessel:	n/a
10	chr7:70254810-70254860	HCM	heart:	n/a
11	chr7:70255210-70255260	ECC-1	luminal epithelium:	n/a
12	chr7:70252953-70253003	NH-A	brain:	n/a
13	chr7:70255210-70255260	HIPEpiC	eye:	n/a
14	chr7:70258010-70258060	HEK293	kidney:	embryo
15	chr7:70311321-70311371	GM12891	blood:	n/a
16	chr7:70258010-70258060	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:70252282-70252332	HRCEpiC	kidney:	n/a
18	chr7:70252448-70252498	NHBE	bronchial:	n/a
19	chr7:70255985-70256035	HCT-116	colon:	n/a
20	chr7:70258649-70258699	MCF-7	breast:	n/a
21	chr7:70255332-70255382	HRCEpiC	kidney:	n/a
22	chr7:70257960-70258010	HCF	heart:	n/a
23	chr7:70255985-70256035	SAEC	small airway:	n/a
24	chr7:70258753-70258803	HRPEpiC	eye:	n/a
25	chr7:70258753-70258803	AG09309	skin:	n/a
26	chr7:70255416-70255466	IMR90	lung:	fetal
27	chr7:70255210-70255260	HCT-116	colon:	n/a
28	chr7:70311321-70311371	MCF10A-Er-Src	breast:	n/a
29	chr7:70252282-70252332	BE2_C	brain:	n/a
30	chr7:70252448-70252498	SKMC	muscle:	n/a
31	chr7:70252448-70252498	PANC-1	pancreas:	n/a
32	chr7:70252448-70252498	AG10803	skin:	n/a
33	chr7:70257960-70258010	GM12878	blood:	n/a
34	chr7:70294511-70294561	A549	lung:	n/a
35	chr7:70294525-70294575	HEK293	kidney:	embryo
36	chr7:70255332-70255382	GM12878	blood:	n/a
37	chr7:70311532-70311582	AG09309	skin:	n/a
38	chr7:70256003-70256053	HCT-116	colon:	n/a
39	chr7:70294525-70294575	GM19239	blood:	n/a
40	chr7:70252662-70252712	H1-hESC	embryonic stem cell:	embryo
41	chr7:70294264-70294314	CMK	blood:	n/a
42	chr7:70258726-70258776	HEEpiC	esophagus:	n/a
43	chr7:70294511-70294561	HCM	heart:	n/a
44	chr7:70252662-70252712	SK-N-SH	brain:	n/a
45	chr7:70311435-70311485	SK-N-SH_RA	brain:	n/a
46	chr7:70255804-70255854	H1-hESC	embryonic stem cell:	embryo
47	chr7:70257960-70258010	HCT-116	colon:	n/a
48	chr7:70255332-70255382	Hela-S3	cervix:	n/a
49	chr7:70257960-70258010	HIPEpiC	eye:	n/a
50	chr7:70252335-70252385	HEEpiC	esophagus:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
2	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
3	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
4	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
5	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
6	chr7:69997760..70000305-chr7:70252452..70255075,2	MCF-7	breast:
7	chr7:70244569..70247076-chr7:70250539..70253250,4	K562	blood:
8	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
9	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
10	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
11	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
12	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
13	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
14	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
15	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
16	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
AUTS2	TF binding region
ENSG00000236978	TF binding region
AUTS2	CpG island
ENSG00000236978	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 2715 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2715 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12698936	chr7:70249358-70249359	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34521401	chr7:70249362-70249363	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs62456836	chr7:70249363-70249364	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571963042	chr7:70249367-70249368	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556673266	chr7:70249368-70249369	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs578168679	chr7:70249425-70249426	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10228883	chr7:70249445-70249446	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549639703	chr7:70249468-70249469	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537881843	chr7:70249479-70249480	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs187601608	chr7:70249488-70249489	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs112992753	chr7:70249503-70249504	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs527686385	chr7:70249517-70249518	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192871711	chr7:70249560-70249561	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542910172	chr7:70249615-70249616	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561663773	chr7:70249645-70249646	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs531782507	chr7:70249646-70249647	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs549986826	chr7:70249660-70249661	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532597100	chr7:70249681-70249682	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532838484	chr7:70249687-70249688	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs569394259	chr7:70249688-70249689	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs9886083	chr7:70249707-70249708	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566306290	chr7:70249721-70249722	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs542963117	chr7:70249750-70249751	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs576131651	chr7:70249751-70249752	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs71530329	chr7:70249753-70249754	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs553945769	chr7:70249756-70249757	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs533825973	chr7:70249758-70249759	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs9886311	chr7:70249760-70249761	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555372047	chr7:70249811-70249812	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567595527	chr7:70249841-70249842	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs139250024	chr7:70249867-70249868	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3817575	chr7:70249868-70249869	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs368372534	chr7:70249879-70249880	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs559562433	chr7:70249880-70249881	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs372241813	chr7:70249904-70249905	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs2293504	chr7:70249908-70249909	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539087101	chr7:70249909-70249910	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs142157196	chr7:70249963-70249964	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs34479874	chr7:70249984-70249985	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199704244	chr7:70249994-70249995	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373111947	chr7:70250013-70250014	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs375051158	chr7:70250024-70250025	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369080848	chr7:70250036-70250037	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs78343289	chr7:70250087-70250088	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs28606546	chr7:70250109-70250110	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs2293503	chr7:70250125-70250126	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs561398631	chr7:70250128-70250129	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576360033	chr7:70250169-70250170	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs543731021	chr7:70250179-70250180	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs566478345	chr7:70250198-70250199	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70214800-70250000	Weak transcription	Psoas Muscle	Psoas
2	chr7:70222000-70258000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:70226400-70254800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:70227400-70253000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:70228000-70249400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:70228400-70250000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:70228400-70257400	Weak transcription	Right Atrium	heart
8	chr7:70229400-70259600	Strong transcription	Fetal Muscle Trunk	muscle
9	chr7:70229400-70259600	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr7:70230200-70254000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:70230200-70257400	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr7:70230600-70250000	Weak transcription	Right Ventricle	heart
13	chr7:70231000-70250000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:70231600-70250000	Weak transcription	NHLF	lung
15	chr7:70232000-70250000	Weak transcription	Pancreas	Pancrea
16	chr7:70232000-70250000	Weak transcription	HMEC	breast
17	chr7:70233400-70250200	Weak transcription	Colonic Mucosa	Colon
18	chr7:70234600-70259600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:70235200-70258200	Strong transcription	HSMMtube	muscle
20	chr7:70236400-70250000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:70236400-70257000	Strong transcription	Skeletal Muscle Male	skeletal muscle
22	chr7:70236800-70258200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:70237800-70249800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:70237800-70249800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:70238400-70250000	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:70238600-70259600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr7:70238800-70259600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:70239200-70259400	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr7:70239800-70259400	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr7:70240200-70257000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:70240200-70258000	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr7:70240800-70259200	Strong transcription	Fetal Intestine Small	intestine
33	chr7:70241000-70259200	Strong transcription	Aorta	Aorta
34	chr7:70241200-70257200	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:70241400-70256400	Strong transcription	Stomach Smooth Muscle	stomach
36	chr7:70241400-70257400	Strong transcription	HSMM	muscle
37	chr7:70241800-70257200	Strong transcription	H9 Cell Line	embryonic stem cell
38	chr7:70241800-70259400	Strong transcription	Duodenum Mucosa	Duodenum
39	chr7:70242000-70252600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:70242000-70257200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:70242200-70249600	Weak transcription	Osteobl	bone
42	chr7:70242200-70250000	Weak transcription	Fetal Heart	heart
43	chr7:70242200-70259600	Strong transcription	Dnd41	blood
44	chr7:70242200-70259600	Weak transcription	NHDF-Ad	bronchial
45	chr7:70242600-70249600	Weak transcription	Spleen	Spleen
46	chr7:70242600-70249800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:70242600-70250400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr7:70243000-70249800	Weak transcription	Small Intestine	intestine
49	chr7:70243200-70249400	Weak transcription	Brain Substantia Nigra	brain
50	chr7:70243200-70259600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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